MYLOTARG
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Manufactured by Pfizer
*You can pay as little as $0 per fill using Drug Coupons or Patient Assistance Programs. Subject to applicability & eligibility requirements.
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MYLOTARG Uses, Side Effects, Interactions, Warnings & Dosing
What is MYLOTARG?
MYLOTARG is the brand name for gemtuzumab ozogamicin and is available as an injection for IV use.
What dosages is MYLOTARG available in?
MYLOTARG is available as a 4.5 mg IV injection.
What is MYLOTARG used for?
MYLOTARG is an antibody-drug conjugate and is used for the following:
- Newly-diagnosed acute myeloid leukemia (AML) that’s
- CD33-positive in adults and children 1 month or older
- Previously-treated acute myeloid leukemia (AML) that’s
- CD33-positive in adults and children 2 years and older
How does MYLOTARG work?
MYLOTARG is a type of cancer medication known as an antibody-drug conjugate. It’s made up of two parts: a monoclonal antibody and a chemotherapy drug called calicheamicin. The antibody takes MYLOTARG to acute myeloid leukemia cells in the body that have a specific protein called CD33. Once there, the chemotherapy damages the leukemia cell’s DNA, which kills the cancer cell.
How do I take MYLOTARG?
The dose and treatment schedule depends on your age, your AML status, and whether you’re taking MYLOTARG along with other chemotherapy.
- In general, MYLOTARG is given as an infusion through the vein (IV) by a healthcare provider.
- First-choice treatment for newly-diagnosed AML
Adults
- The dose is based on your body size using body surface area (BSA), which takes into account your weight and height
- When used together with other chemotherapy: A treatment course consists of 1 induction cycle and then 2 consolidation cycles
- Induction cycle: The typical dose is 3 mg/m2 given IV on days 1, 4 and 7
- Consolidation cycles: The typical dose is 3 mg/m2 given IV on day 1.
- When used by itself: A treatment course consists of 1 induction cycle and up to 8 consolidation cycles
- Induction cycle: The typical dose is 6 mg/m2 given IV on day 1 and then 3 mg/m2 given IV on day 8
- Consolidation cycles: The typical dose is 2 mg/m2 given IV on day 1 every 4 weeks
- Children 1 month and older: Treatment days vary based on the treatment protocol that the healthcare team is following. The dose is based on body size, either using body surface area (mg/m2) or using body weight (mg/kg)
- Previously-treated AML
- People 2 years and older: The typical dose is 3 mg/m2 given IV on days 1, 4, and 7 for one course of treatment
Is it safe for me to take MYLOTARG?
MYLOTARG is a safe and effective treatment when used for FDA licensed indications. However, like all medications, they may give you unwanted side effects. You should always discuss potential side effects with your physician to ensure the medication is suitable and right for you.
MYLOTARG Common Side Effects
Common side effects of MYLOTARG:
- Fever
- Liver problems
- Tiredness
- Infection
- Heart problems
- Bleeding
- Nausea and vomiting
- Constipation
- Mouth sores
MYLOTARG Serious Side Effects
Serious side effects are rare with MYLOTARG. Contact your healthcare provider immediately if you experience any of the following.
- Serious liver problems: swollen belly, sudden weight gain, yellow skin, yellow eyes, stomach pain
- Bleeding: nosebleeds, blood in stool, unexplained bruising, blood in urine, sudden headache
- Infusion-related reactions: fever, fast heart rate, chills, trouble breathing, low blood pressure
Effects of other drugs, drug classes and over-the-counter products on MYLOTARG
There are no major drug interactions listed for MYLOTARG. However, always let your physician and pharmacist know about any other medications or supplements (including prescribed and over-the-counter medications, vitamins, and dietary or herbal supplements) that you are currently taking.
Who makes MYLOTARG?
Pfizer
Is MYLOTARG safe in pregnancy?
Based on its mechanism of action and findings from animal studies, MYLOTARG can cause embryo-fetal harm when administered to a pregnant woman. Females who can become pregnant should use effective contraception during treatment with MYLOTARG and for at least 6 months after the final dose. Males with female partners of reproductive potential to use effective contraception during treatment with MYLOTARG and for at least 3 months after the last dose.
The FDA's medical product safety reporting program for health professionals, patients and consumers.
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Medical Disclaimer
NowPatient has taken all reasonable steps to ensure that all material is factually accurate, complete, and current. However, the knowledge and experience of a qualified healthcare professional should always be sought after instead of using the information on this page. Before taking any drug, you should always speak to your doctor or another qualified healthcare provider.
The information provided here about medications is subject to change and is not meant to include all uses, precautions, warnings, directions, drug interactions, allergic reactions, or negative effects. The absence of warnings or other information for a particular medication does not imply that the medication or medication combination is appropriate for all patients or for all possible purposes.
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